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Pharmaceuticals Lonza, Sanquin Collaborate for Commercialisation of Specialised Reagents

| Editor: Ahlam Rais

Under a strategic partnership, Lonza and Sanquin will work together for the commercialisation of a range of specialised reagents for pyrogen testing of parenteral pharmaceuticals and medical devices using the Monocyte Activation Test.

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The partnership will enable drug developers to explore the full potential of the MAT method to bring safe pharmaceuticals to the market.
The partnership will enable drug developers to explore the full potential of the MAT method to bring safe pharmaceuticals to the market.
(Source: Deposit Photos)

Basel/Switzerland – Lonza Sales, through its Bioscience Division, and Sanquin Reagents have entered into a strategic partnership for the commercialisation of a range of specialised reagents for pyrogen testing of parenteral pharmaceuticals and medical devices using the Monocyte Activation Test (MAT). This partnership expands Lonza’s extensive portfolio of endotoxin testing products, and enables drug developers and quality control (QC) laboratories to explore the full potential of the high-performing, sustainable MAT method to bring safe pharmaceuticals to the market.

Contrary to the conventional Rabbit Pyrogen Test (RPT), which works by measuring temperature changes in rabbits following administration of a test sample, the MAT does not involve the use of experimental animals. As such, it enables QC laboratories to comply with stringent animal welfare regulations and meet their sustainability objectives. Being a highly sensitive in vitro human cell-based assay, the MAT is capable of consistently detecting pyrogenic activity in even the most complex pharmaceuticals, such as vaccines and cell- and antibody-based biologics, where use of the RPT is limited.

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Under the new agreement between Lonza and Sanquin, cryopreserved pooled human Peripheral Blood Mononuclear Cells (PBMCs) produced by Sanquin specifically for use with the MAT will bear the Lonza branding. The cells are developed in line with the requirements of the European Pharmacopoeia chapter 2.6.30, following an optimised donor selection, cell isolation and cell quality testing process.

Compared to fresh PBMCs, cryopreserved pooled PBMCs eliminate the need to undertake cell isolation for each single test run. As a result, the cells are available on demand whenever a need arises and large number of vials from one batch guarantees a long term test consistency. Lonza will further distribute the Sanquin-branded Peli Kine compact Elisa Kits that have been validated for use with the MAT assay. Together with Lonza’s testing hardware, media and accessory offering, drug developers and QC laboratories will now profit from a comprehensive and optimised MAT solution that is in line with regulatory requirements.

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